Prednisone
- Product NDC
- 70518-3142
- 11-digit product format
- 705183142
- Labeler code
- 70518
- Product ID
- 70518-3142_d2cc6d86-7c06-5ec1-e053-2995a90ae079
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211575
- Marketing category
- ANDA
- Marketing start
- 2021-07-05
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3142 | PREDNISONE TABLET [REMEDYREPACK INC.] | 8 | Legacy NDC | 20240926_9e2bd1de-e759-46e0-a12f-734660e8e8bf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3142-0 | 70518314200 | 30 TABLET in 1 BLISTER PACK (70518-3142-0) | 30 tablet | 2021-07-05 | 0000-00-00 | No | No | Current |
| 70518-3142-1 | 70518314201 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-3142-1) | 180 tablet | 2021-09-24 | 0000-00-00 | No | No | Current |
| 70518-3142-2 | 70518314202 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-3142-2) | 180 tablet | 2021-12-09 | 0000-00-00 | No | No | Current |